##  [Support in Filing Initial CEP and CEP-LCM Submissions with Zero Errors](/index%2ephp/case-studies/support-in-filing-initial-cep-and-cep-lcm-submissions-with-zero-errors) 

- [Medicinal Products](/index%2ephp/case-studies-main-categories/medicinal-products)
- [Publishing and Submission](/index%2ephp/case-studies-main-categories/publishing-and-submission)





[European Medicines Agency](/index%2ephp/case-studies-heath-authority/european-medicines-agency)

 

 ![Support in Filing Initial CEP and CEP-LCM Submissions with Zero Errors]()

A Belgium-based multinational chemical company was looking for Regulatory support in the filing of Initial CEP and CEP-LCM Submissions to the EMA. The project came with several challenges, such as:

- Reviewing all the source documents
- Working on large volumes of documents
- Taking care of end-to-end publishing activities

Under rigid timelines and with last-minute submission requests, Freyr took up the challenge and filed the submissions with zero errors and warnings. Freyr’s experts tracked all the version changes made in the documents throughout the publishing cycle.

Learn how Freyr achieved 100% success in filing ad hoc submissions to the EMA with zero errors and warnings. Download the proven case.



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